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Chlorinated plastoquinone analogs that inhibit Staphylococcus epidermidis and Candida albicans growth
EM. Kara, N. Bayrak, H. Yıldırım, M. Yıldız, BO. Celik, AF. Tuyun
Language English Country United States
Document type Journal Article
Grant support
FBA-2016-20662
the Scientific Research Projects Coordination Unit of Istanbul University-Cerrahpasa
- MeSH
- Anti-Infective Agents chemistry pharmacology MeSH
- Biofilms drug effects growth & development MeSH
- Candida albicans drug effects growth & development MeSH
- Halogenation MeSH
- Microbial Sensitivity Tests MeSH
- Molecular Structure MeSH
- Plastoquinone analogs & derivatives chemistry pharmacology MeSH
- Staphylococcus epidermidis drug effects growth & development MeSH
- Structure-Activity Relationship MeSH
- Publication type
- Journal Article MeSH
Infectious diseases are the significant global health problem because of drug resistance to most classes of antimicrobials. Interest is growing in the development of new antimicrobials in pharmaceutical discovery. For that reason, the urgency for scientists to find and/or develop new important molecules is needed. Many natural active molecules that exhibit various biological activities have been isolated from the nature. For the present research, a new selected set of aminobenzoquinones, denoted as plastoquinone analogs (PQ1-24), was employed for their in vitro antimicrobial potential in a panel of seven bacterial strains (three Gram-positive and four Gram-negative bacteria) and three fungi. The results revealed PQ analogs with specific activity against bacteria including Staphylococcus epidermidis and pathogenic fungi, including Candida albicans. PQ8 containing methoxy group at the ortho position on the phenylamino moiety exhibited the highest growth inhibition against S. epidermidis with a minimum inhibitory concentration of 9.76 μg/mL. The antifungal profile of all PQ analogs indicated that five analogs (while PQ1, PQ8, PQ9, PQ11, and PQ18 were effective against Candida albicans, PQ1 and PQ18 were effective against Candida tropicalis) have potent antifungal activity. Selected analogs, PQ1 and PQ18, were studied for biofilm evaluation and time-kill kinetic study for better understanding.
Chemistry Department Gebze Technical University Gebze 41400 Kocaeli Turkey
Department of Chemistry Faculty of Science Istanbul University Vezneciler 34134 Istanbul Turkey
References provided by Crossref.org
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